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01 1Alginic Acid Alumina; Hydrated Sodium Bicarbonate
02 1Alginsyre; Aluminium Hydroxide; Sodium Hydrogen Carbonate
03 2Allopurinol
04 1Alumina, Hydrated; Calcium Carbonate; Sodium Alginate; Sodium Bicarbonate
05 1Aluminium Hydroxide Gel; Calcium Carbonate; Sodium Hydrogen Carbonate
06 2Amiloride Hydrochloride Dihydrate; Hydrochlorothiazide
07 1Apricot
08 1Aprotinin
09 1Aprotinin, Bovint
10 1Cetirizine Dihydrochloride
11 2DESMOPRESSIN ACETATE
12 3Desloratadine
13 5Dexibuprofen
14 1Docetaxel
15 1Docetaxel (Vattenfri)
16 1Doxycycline Hyclate
17 1Doxycycline Monohydrate
18 4Gimeracil; Oteracil Potassium; Tegafur
19 1Glucosamine Sulfate Potassium Chloride
20 1Loperamide Hydrochloride
21 1Loperamide Hydrochloride; Simethicone
22 8METHOTREXATE
23 75Metadonhydroklorid
24 80Methotrexate
25 8Methotrexate Disodium
26 8Metotreksat
27 1Misoprostol
28 2My Firstborn
29 5Naloxone Hydrochloride Dihydrate; Oxycodone Hydrochloride
30 2Paracetamol
31 2Ranitidine Hydrochloride
32 1Sodium Hyaluronate
33 1Sodium Picosulfate (Monohydrate)
34 2Sodium alginate; Aluminum hydroxide; Sodium hydrogen carbonate
35 3Sodium alginate; Aluminum hydroxide; Sodium hydrogen carbonate; Calcium carbonate
36 4Tegafur; Gimeracil; Oteracilmonokalium
37 2Tegafur; Gimeracil; Oteracil
38 4Tegafur; Gimeracil; Oteracyl Potassium
39 1Terbinafinhydrochloride
40 3Xylometazoline Hydrochloride
41 4Ziprasidone Hydrochloride (Anhydrous)
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01 3Disphar International Bv
02 8NORDIC GRP
03 2NORDIC PHARMA
04 55Nordic Drugs AB
05 59Nordic Drugs Ab
06 36Nordic Group B.V.
07 12Nordic Group BV
08 50Nordic Group Bv
09 4Nordic Pharma Bv
10 20Nordic Pharma Gmbh
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01 12Capsule
02 4Chewable Tablet
03 3Concentrate For Solution For Infusion
04 2Effervescent Tablet
05 11Film Coated Tablet
06 1Granules
07 4Hard Capsule
08 2Hard Capsules
09 2INJECTABLE;INJECTION
10 3Inhalation Spray
11 4Injectable Solution
12 8Injectable Solution In Pre-Filled Pen
13 8Injectable Solution In Pre-Filled Syringe
14 1Injection/Infusion Solution
15 1Oral Drops
16 25Oral Solution
17 5Oral Suspension
18 8SOLUTION;SUBCUTANEOUS
19 77Solution For Injection
20 2Solution For Injection/Infusion
21 50Syrup
22 16Tablet
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01 10.004MG/ML
02 10.015MG/ML
03 10.5mg/ml
04 110.0mg/0.4ml
05 110000 KIE/ml
06 110000KIE/ml
07 5100mg
08 210MG
09 110MG/0.4ML (10MG/0.4ML)
10 1010mg
11 310mg/0.4ml
12 110mg/ml
13 110mg;5mg
14 3110mg
15 212.5MG
16 112.5MG/0.5ML (12.5MG/0.5ML)
17 612.5mg
18 212.5mg/0.5ml
19 3120mg
20 2125mg/0.5ml
21 3130mg
22 3140mg
23 115.0mg/0.6ml
24 4150mg
25 215MG
26 115MG/0.6ML (15MG/0.6ML)
27 215MG; 4.35MG; 11.8 MG
28 915mg
29 315mg/0.6ml
30 315mg; 4.35mg; 11.8mg
31 115mg; 435mg; 118mg
32 115mg;4.35mg;11.8mg
33 3160mg
34 217.5MG
35 117.5MG/0.7ML (17.5MG/0.7ML)
36 617.5mg
37 217.5mg/0.7ml
38 3170mg
39 2175mg/0.7ml
40 3180mg
41 3190mg
42 21mg/ml
43 12.5mg;25mg
44 120.0mg/0.8ml
45 5200mg
46 220MG
47 120MG/0.8ML (20MG/0.8ML)
48 220MG; 5.8MG; 15.8 MG
49 1020mg
50 320mg/0.8ml
51 320mg/ml
52 320mg; 5.8mg; 15.8mg
53 120mg; 58mg; 158mg
54 120mg;10mg
55 120mg;5.8mg;15.8mg
56 222.5MG
57 122.5MG/ML (22.5MG/ML)
58 622.5mg
59 222.5mg/0.9ml
60 2225mg/0.9ml
61 1250mg
62 225MG
63 125MG/1ML (25MG/1ML)
64 925mg
65 125mg/1.0ml
66 325mg/ml
67 12mg
68 130 mg;15 mg
69 4300mg
70 330mg
71 335mg
72 1400mcg
73 2400mg
74 440mg
75 140mg;20mg
76 345mg
77 2500mg
78 350mg
79 355mg
80 1595mg
81 35mg
82 15mg;2.5mg
83 15mg;50mg
84 1600mg
85 460mg
86 27.5MG
87 17.5MG/0.3ML (7.5MG/0.3ML)
88 67.5mg
89 27.5mg/0.3ml
90 17.5mg/ml
91 370mg
92 275mg/0.3ml
93 480mg
94 390mg
95 11Blank
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01 24Denmark
02 18Estonia
03 67Norway
04 20Spain
05 90Sweden
06 20Switzerland
07 10USA
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Regulatory Info : Approved
Registration Country : Sweden
Alginic Acid Alumina; Alginic Acid Alumina; Hydrated Sodium Bicarbonate
Dosage Form : Chewable Tablet
Brand Name : Gaviscon
Dosage Strength :
Packaging :
Approval Date : 30-08-1974
Application Number : 1.97E+13
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Prescription
Registration Country : Denmark
Alginsyre; Aluminium Hydroxide; Sodium Hydrogen Carbonate
Dosage Form : Chewable Tablet
Brand Name : Gaviscon
Dosage Strength :
Packaging :
Approval Date : 05-09-1975
Application Number : 28100656774
Regulatory Info : Prescription
Registration Country : Denmark

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Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Tablet
Brand Name : Allopurinol Nordic Drugs
Dosage Strength : 100mg
Packaging :
Approval Date : 25-01-1991
Application Number : 1.99E+13
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Tablet
Brand Name : Allopurinol Nordic Drugs
Dosage Strength : 300mg
Packaging :
Approval Date : 25-01-1991
Application Number : 1.99E+13
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Approved
Registration Country : Sweden
Alumina, Hydrated; Calcium Carbonate; Sodium Alginate; Sodium Bicarbonate
Dosage Form : Oral Suspension
Brand Name : Gaviscon
Dosage Strength :
Packaging :
Approval Date : 05-02-1982
Application Number : 1.98E+13
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Prescription
Registration Country : Denmark
Aluminium Hydroxide Gel; Calcium Carbonate; Sodium Hydrogen Carbonate
Dosage Form : Oral Suspension
Brand Name : Gaviscon
Dosage Strength :
Packaging :
Approval Date : 01-09-1982
Application Number : 28101082281
Regulatory Info : Prescription
Registration Country : Denmark

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Regulatory Info : Approved
Registration Country : Sweden
Amiloride Hydrochloride Dihydrate; Hydrochlorothiazide
Dosage Form : Tablet
Brand Name : Amyloferm
Dosage Strength : 5mg;50mg
Packaging :
Approval Date : 04-05-1990
Application Number : 1.99E+13
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Approved
Registration Country : Sweden
Amiloride Hydrochloride Dihydrate; Hydrochlorothiazide
Dosage Form : Tablet
Brand Name : Amyloferm Mite
Dosage Strength : 2.5mg;25mg
Packaging :
Approval Date : 04-05-1990
Application Number : 1.99E+13
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Allowed
Registration Country : Switzerland
Dosage Form : Solution For Injection/I...
Brand Name : Trasylol
Dosage Strength :
Packaging :
Approval Date : 16/03/1977
Application Number : 38837
Regulatory Info : Allowed
Registration Country : Switzerland

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Regulatory Info : Prescription
Registration Country : Denmark
Dosage Form : Injection/Infusion Solut...
Brand Name : Trasylol
Dosage Strength : 10000 KIE/ml
Packaging :
Approval Date : 04-07-1990
Application Number : 28101385789
Regulatory Info : Prescription
Registration Country : Denmark
